Skip to content

Gold Dental Casting Alloys

by Bego U.S.A. 510(k)

Active United States

510(k) K033279

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK033279 Date15 Jan 2004ClearedStatusActive

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
EJT
Device Class
Class II
Regulation
21 CFR Part 872.3060
Advisory Committee
Dental
FDA Decision
SESE Substantially Equivalent

Other devices from Bego U.S.A.

  • Wirobond C

    Class II

  • Aurolloyd Kf

    Class II

  • Begopal

    Class II

  • Bio PontoStar

    Class II

  • Platinlloyd 100

    Class II

  • Begocer G

    Class II